A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840075



Internal ID22615010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6546627..6558222hg38UCSC Ensembl
chr4:6548354..6559949hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3811596
hg1911596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497109
Samples
Known GenesPPP2R2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840075
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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